石墨氮化碳
锂(药物)
金属锂
电解质
材料科学
金属
氮化物
碳纤维
接触电阻
石墨烯
电极
纳米技术
化学工程
化学
催化作用
物理化学
复合材料
图层(电子)
冶金
医学
生物化学
光催化
复合数
工程类
内分泌学
作者
Ying Huang,Bo Chen,Jian Duan,Fei Yang,Tengrui Wang,Zhengfeng Wang,Wenjuan Yang,Chenchen Hu,Wei Hua Luo,Yunhui Huang
标识
DOI:10.1002/ange.201914417
摘要
Abstract Solid‐state Li metal batteries (SSLMBs) have attracted considerable interests due to their promising energy density as well as high safety. However, the realization of a well‐matched Li metal/solid‐state electrolyte (SSE) interface remains challenging. Herein, we report g‐C3N4 as a new interface enabler. We discover that introducing g‐C3N4 into Li metal can not only convert the Li metal/garnet‐type SSE interface from point contact to intimate contact but also greatly enhance the capability to suppress the dendritic Li formation because of the greatly enhanced viscosity, decreased surface tension of molten Li, and the in situ formation of Li3N at the interface. Thus, the resulting Li‐C3N4|SSE|Li‐C3N4 symmetric cell gives a significantly low interfacial resistance of 11 Ω cm2 and a high critical current density (CCD) of 1500 μA cm−2. In contrast, the same symmetric cell configuration with pristine Li metal electrodes has a much larger interfacial resistance (428 Ω cm2) and a much lower CCD (50 μA cm−2).
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